Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elmer Balajonda"'
Autor:
Alan Sugar, MD, Munira Hussain, MS, Winston Chamberlain, MD, PhD, Reza Dana, MD, David Patrick Kelly, MD, Christopher Ta, MD, John Irvine, MD, Melissa Daluvoy, MD, Victor Perez, MD, Joshua Olson, MD, Vishal Jhanji, MD, Terence A. Walts, MBA, Robert Doyle Stulting, MD, PhD, Edmund K. Waller, MD, PhD, Neera Jagirdar, MD, MPH, Shahzad Mian, MD, Roni Shtein, MD, H. Kaz Soong, MD, Munira Hussain, Afshan Nanji, MD, MPH, John Clements, MD, Jennifer Maykovski, Paula Cisternas Labadzinzki, Jia Jin, MD, Joseph Ciolino, MD, John Caccaviello, D. Patrick Kelly, MD, Roya Habibi, OD, Charles Yu, MD, Charles Lin, MD, Kristin Hirabayashi, MD, Gabriel Valerio, MD, Supriya Kawale, Mariana Nunez, Olivia Lee, MD, Matthew Chu, Elmer Balajonda, Terry Hawks, Amanda Maltry, MD, Joshua Hou, MD, Wendy Elasky, Rose Carla Aubourg, R. Doyle Stulting, MD, PhD, Edmund Waller, MD, PhD, Neera Jagirdar, MD, Terence Walts
Publikováno v:
Ophthalmology Science, Vol 2, Iss 3, Pp 100176- (2022)
Purpose: The purpose of the study was to evaluate, as a pilot trial, safety and tolerability of CAM-101 10% and 30% topical ophthalmic fibrinogen-depleted human platelet lysate (FD hPL) solution in patients with dry eye disease (DED) secondary to gra
Externí odkaz:
https://doaj.org/article/11da6f8f0e9a445cb5f5eaa1c938aad7
Autor:
Natalie A. Afshari, Robert P. Igo, Nathan J. Morris, Dwight Stambolian, Shiwani Sharma, V. Lakshmi Pulagam, Steven Dunn, John F. Stamler, Barbara J. Truitt, Jacqueline Rimmler, Abraham Kuot, Christopher R. Croasdale, Xuejun Qin, Kathryn P. Burdon, S. Amer Riazuddin, Richard Mills, Sonja Klebe, Mollie A. Minear, Jiagang Zhao, Elmer Balajonda, George O. Rosenwasser, Keith H Baratz, V. Vinod Mootha, Sanjay V. Patel, Simon G. Gregory, Joan E. Bailey-Wilson, Marianne O. Price, Francis W. Price, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi-Ju Li, Sudha K. Iyengar
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Fuchs endothelial corneal dystrophy (FECD) is one of the most common reasons for corneal transplantation, and is known to cluster in families. Here, the authors discover new genetic loci associated with FECD with sex-specific effects and implications
Externí odkaz:
https://doaj.org/article/d1c65f3362014583bd22c5188abefc76
Autor:
Yi-Ju Li, Mollie A Minear, Jacqueline Rimmler, Bei Zhao, Elmer Balajonda, Michael A Hauser, R Rand Allingham, Allen O Eghrari, S Amer Riazuddin, Nicholas Katsanis, John D Gottsch, Simon G Gregory, Gordon K Klintworth, Natalie A Afshari
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e18044 (2011)
Fuchs endothelial corneal dystrophy (FECD) is a common, late-onset disorder of the corneal endothelium. Although progress has been made in understanding the genetic basis of FECD by studying large families in which the phenotype is transmitted in an
Externí odkaz:
https://doaj.org/article/6728000597c34a7097af38dd6639c715
Autor:
Kathryn P. Burdon, Marianne O. Price, Natalie A. Afshari, Simon G. Gregory, Jiagang Zhao, S. Amer Riazuddin, Sanjay V. Patel, Elmer Balajonda, Sudha K. Iyengar, Christopher R. Croasdale, Jamie E Craig, Venkateswara Mootha, Gordon K. Klintworth, Barbara Truitt, John F. Stamler, George O D Rosenwasser, Shiwani Sharma, Abraham Kuot, Jonathan H. Lass, Mollie A. Minear, Richard A. Mills, Steven P. Dunn, Sonja Klebe, Keith H. Baratz, John H. Fingert, Anthony J. Aldave, Xuejun Qin, Dwight Stambolian, V. Lakshmi Pulagam, John D. Gottsch, Joan E. Bailey-Wilson, Francis W. Price, Nathan Morris, Yi-Ju Li, Robert P. Igo, J. B. Rimmler
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Nature Communications
Nature Communications
The structure of the cornea is vital to its transparency, and dystrophies that disrupt corneal organization are highly heritable. To understand the genetic aetiology of Fuchs endothelial corneal dystrophy (FECD), the most prevalent corneal disorder r
Autor:
Mollie A, Minear, Yi-Ju, Li, Jacqueline, Rimmler, Elmer, Balajonda, Shera, Watson, R Rand, Allingham, Michael A, Hauser, Gordon K, Klintworth, Natalie A, Afshari, Simon G, Gregory
Publikováno v:
Molecular Vision
Purpose Fuchs endothelial corneal dystrophy (FECD) is a genetically heterogeneous disorder that has been primarily studied in patients of European or Asian ancestry. Given the sparse literature on African Americans with FECD, we sought to characteriz
Autor:
Natalie A. Afshari, Gordon K. Klintworth, Simon G. Gregory, Elmer Balajonda, R. Rand Allingham, S. Amer Riazuddin, John D. Gottsch, Nicholas Katsanis, Michael A. Hauser, Bei Zhao, Yi-Ju Li, J. B. Rimmler, Mollie A. Minear, Allen O. Eghrari
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 4, p e18044 (2011)
PLoS ONE, Vol 6, Iss 4, p e18044 (2011)
Fuchs endothelial corneal dystrophy (FECD) is a common, late-onset disorder of the corneal endothelium. Although progress has been made in understanding the genetic basis of FECD by studying large families in which the phenotype is transmitted in an